Canonical Allele Identifier: CA507537585

Gene: CYP2B6

Linked Data

• MyVariant Identifiers: chr19:g.41518252A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41012347A>T , CM000681.2:g.41012347A>T	GRCh38
NC_000019.9:g.41518252A>T , CM000681.1:g.41518252A>T	GRCh37
NC_000019.8:g.46210092A>T	NCBI36
NG_007929.1:g.26049A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324071.10:c.1014A>T MANE Select	ENSP00000324648.2:p.Pro338=
ENST00000598834.2:c.1038A>T
ENST00000324071.8:c.1014A>T	ENSP00000324648.2:p.Pro338=
ENST00000593831.1:c.306A>T	ENSP00000470582.1:p.Pro102=
ENST00000597612.1:n.509A>T
NM_000767.4:c.1014A>T	NP_000758.1:p.Pro338=
XM_005258569.3:c.1014A>T	XP_005258626.1:p.Pro338=
XM_006723050.2:c.1014A>T	XP_006723113.1:p.Pro338=
XM_011526546.1:c.1014A>T	XP_011524848.1:p.Pro338=
XM_011526547.1:c.1014A>T	XP_011524849.1:p.Pro338=
XM_011526548.1:c.534A>T	XP_011524850.1:p.Pro178=
XM_011526549.1:c.423A>T	XP_011524851.1:p.Pro141=
XM_011526550.1:c.414A>T	XP_011524852.1:p.Pro138=
NM_000767.5:c.1014A>T MANE Select	NP_000758.1:p.Pro338=